Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/G/T | Ancestral: C | Ambiguity code: B

Chromosome 7:151080751 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 28 HGVS names - Show

About this variant

This variant overlaps 62 transcripts and 1 regulatory feature.

Variant displays